A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697161



Internal ID15433813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:35514718..35537460hg38UCSC Ensembl
Innerchr17:33841737..33864479hg19UCSC Ensembl
Innerchr17:30865850..30888592hg18UCSC Ensembl
Innerchr17:30865850..30888592hg17UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3822743
hg1922743
hg1822743
hg1722743
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519981
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697161
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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